Canonical Allele Identifier: CA1419602466

Gene: MYNN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784708G= , CM000665.2:g.169784708G=	GRCh38
NC_000003.11:g.169502496G= , CM000665.1:g.169502496G=	GRCh37
NC_000003.10:g.170985190G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1570G= MANE Select	ENSP00000326240.4:p.Gly524=
ENST00000349841.9:c.1570G=	ENSP00000326240.4:p.Gly524=
ENST00000356716.8:c.1570G=	ENSP00000349150.3:p.Gly524=
ENST00000544106.5:c.1483+1148G=	ENSP00000440637.1:n.1483+1148G=
ENST00000602751.5:c.*1178G=	ENSP00000473654.1:n.*1178G=
NM_001185118.1:c.1570G=	NP_001172047.1:p.Gly524=
NM_001185119.1:c.1483+1148G=	NP_001172048.1:n.1483+1148G=
NM_018657.4:c.1570G=	NP_061127.1:p.Gly524=
NR_033702.1:n.1869G=
NR_033703.1:n.1883G=
XM_005247621.3:c.1486G=	XP_005247678.1:p.Gly496=
XM_005247622.3:c.1324G=	XP_005247679.1:p.Gly442=
XM_005247624.3:c.1228G=	XP_005247681.1:p.Gly410=
XM_011512987.1:c.1570G=	XP_011511289.1:p.Gly524=
XM_011512988.1:c.1570G=	XP_011511290.1:p.Gly524=
XM_005247621.5:c.1486G=	XP_005247678.1:p.Gly496=
XM_005247622.4:c.1324G=	XP_005247679.1:p.Gly442=
XM_005247624.4:c.1228G=	XP_005247681.1:p.Gly410=
XM_017006864.2:c.1570G=	XP_016862353.1:p.Gly524=
XM_017006865.2:c.1144G=	XP_016862354.1:p.Gly382=
XM_017006866.2:c.1144G=	XP_016862355.1:p.Gly382=
XM_017006867.2:c.751G=	XP_016862356.1:p.Gly251=
XM_017006868.2:c.667G=	XP_016862357.1:p.Gly223=
XR_002959552.1:n.3402G=
NM_001185118.2:c.1570G=	NP_001172047.1:p.Gly524=
NM_018657.5:c.1570G= MANE Select	NP_061127.1:p.Gly524=
NR_033702.2:n.1538G=
NR_033703.2:n.1552G=